Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:83568691..83570764-chr7:84108131..84110174,2	K562	blood:

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11975852	0.90[EUR][1000 genomes]
rs13236626	0.90[EUR][1000 genomes]
rs1623312	0.83[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];0.97[TSI][hapmap];0.90[EUR][1000 genomes]
rs1626663	0.90[EUR][1000 genomes]
rs1627397	0.90[EUR][1000 genomes]
rs1639559	0.82[CHB][hapmap];0.89[EUR][1000 genomes]
rs1639582	0.90[EUR][1000 genomes]
rs1639583	0.91[EUR][1000 genomes]
rs2535786	0.82[CHD][hapmap];0.93[EUR][1000 genomes]
rs2691695	0.90[EUR][1000 genomes]
rs3801594	0.85[EUR][1000 genomes]
rs4385417	0.85[EUR][1000 genomes]
rs701311	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs701314	0.82[EUR][1000 genomes]
rs701320	0.83[CHB][hapmap];0.82[CHD][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs797802	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs797804	0.81[CHB][hapmap];0.92[EUR][1000 genomes]
rs797805	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs797816	0.87[EUR][1000 genomes]
rs797820	0.83[CHB][hapmap];0.83[CHD][hapmap];0.89[GIH][hapmap]
rs797822	0.80[EUR][1000 genomes]
rs797826	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs797828	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs797831	0.82[EUR][1000 genomes]
rs797833	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv607707	chr7:83381032-83646816	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv888620	chr7:83459908-83593805	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv888622	chr7:83526743-83631376	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83568600-83572400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:83569800-83571000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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